CLASS II Device recall · Reported 15 Feb 2017 · FDA Enforcement Report

Bariatric Bed - BAR600IVC recalled by Invacare

Invacare is recalling Bariatric Bed - BAR600IVC, distributed in 37 states. The recall was initiated on 2 Dec 2016 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesBAR600IVC

Quantity recalled411 Units

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-1182-2017
FDA event ID: 75939
Recalling firm: Invacare, Elyria, OH
Classification: Class II
Status: Terminated
Recall initiated: 2 Dec 2016
FDA classified: 9 Feb 2017
Reported: 15 Feb 2017
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Other Reasons
Device type: Other Medical Devices

Timeline

2 Dec 2016	Recall initiated by company
9 Feb 2017	Classified by FDA	+69 days
15 Feb 2017	Published in enforcement report	+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

The junction box used in the bariatric bed may emit sparks and result in a fire.

Product as listed by the FDA

Bariatric Bed - BAR600IVC

Where it was distributed

Products were distributed in the following states: AK, AL, AR, CA, CO, CT, FL, HI, ID, IL, IN, KS, LA, MA, MD, ME, MI, MN, MO, MS, NC, NJ, NM, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, and WI. No foreign accounts

Alaska Alabama Arkansas California Colorado Connecticut Florida Hawaii Idaho Illinois Indiana Kansas Louisiana Massachusetts Maryland Maine Michigan Minnesota Missouri Mississippi

Questions about this recall

Is Bariatric Bed - BAR600IVC recalled?

Yes. Invacare recalled Bariatric Bed - BAR600IVC on 2 Dec 2016. The recall is Class II and its status is Terminated. Recall number Z-1182-2017.

Why was it recalled?

The junction box used in the bariatric bed may emit sparks and result in a fire.

Which lots are affected?

BAR600IVC

Where was it sold?

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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